Clinical Chemistry, Vol 18, 1478-1484, Copyright © 1972 by the American Association for Clinical Chemistry

⁶³Ni Complexes in Rabbit Serum and Urine after Injection of ⁶³NiCl₂

¹ Department of Laboratory Medicine, University of Connecticut School of Medicine, Farmington, Conn. 06032.

Radioactive nickel chloride (⁶³NiCl₂) was injected i.v. into rabbits in dosage of 0.24 mg Ni/kg body wt. ⁶³Ni was rapidly cleared from the serum (T_1/2 8.2 h) during the period from 1 h to 2 days after the injection, but slowly (T_1/2 95 h) during the period from 4 to 7 days after the injection. During 24 h after injection of ⁶³NiCl₂, an average of 90% of serum ⁶³Ni was bound to albumin and 10% was ultrafiltrable. Chromatography on Sephadex G-25 demonstrated the presence of five distinct ⁶³Ni complexes (Fractions I to V) in serum ultrafiltrates. During 24 h after injection of ⁶³NiCl₂, an average of 78% of the administered dose of ⁶³Ni was excreted in the urine. Chromatography of the urine on Sephadex G-25 separated three ⁶³Ni complexes, which appeared to have identical chromatographic mobilities as serum Fractions II, III, and V. The chemical identities of the ultrafiltrable ⁶³Ni complexes in serum and urine have not been established, although one (Fraction V) resembles Ni histidine in its chromatographic mobility on Sephadex G-25. This study demonstrates that ultrafiltrable nickel in serum and urine does not exist primarily as free Ni(II), but instead as Ni complexes, and suggests that ultrafiltrable Ni receptors play an important physiological role in nickel homeostasis by serving as diffusible vehicles for the extracellular transport and renal excretion of nickel.

Submitted on August 11, 1972

The following articles in journals at HighWire Press have cited this article:

				F. W. Sunderman JR, A. Aitio, L. G. Morgan, and T. Norseth Biological Monitoring of Nickel Toxicology and Industrial Health, January 1, 1986; 2(1): 17 - 78. [Abstract] [PDF]